Department of Cranio- and Maxillofacial Surgery, University Hospital Regensburg, D-93053 Regensburg, Germany.
Department of Cranio- and Maxillofacial Surgery, University Hospital Regensburg, D-93053 Regensburg, Germany.
Biochem Biophys Res Commun. 2014 Jan 10;443(2):500-4. doi: 10.1016/j.bbrc.2013.11.120. Epub 2013 Dec 7.
Dental follicle cells (DFCs) are dental stem/progenitor cells and the genuine precursors of alveolar osteoblasts and dental cementoblasts. A previous study showed that the transcription factor DLX3 (distal less homeobox 3) supports the osteogenic differentiation in DFCs via a positive feedback loop with the bone morghogenetic protein (BMP) 2. Until today, however, the control of this BMP2/DLX3 pathway by additional signaling pathways remains elusive. Previous studies also suggested that the NOTCH signaling pathway plays a role in the osteogenic differentiation of DFCs. In this study we showed that DLX3 overexpression and the initiation of the osteogenic differentiation by BMP2 or dexamethasone induced the NOTCH signaling pathway in DFCs. However, the induction of NOTCH-signaling impaired not only the osteogenic differentiation (ALP activity and mineralized nodules) but also the expression of the transcription factor DLX3 and the activation of the BMP-signaling pathway. So, NOTCH signaling plays a regulatory role for the osteogenic differentiation of DFCs. In conclusion, results of our study suggest that the NOTCH-signaling pathway, which is activated during the osteogenic differentiation of DFCs, regulates the BMP2/DLX3 directed differentiation of DFCs via a negative feed-back loop.
牙滤泡细胞(DFCs)是牙源性干细胞/祖细胞,是牙槽骨细胞和牙骨质细胞的真正前体细胞。先前的研究表明,转录因子 DLX3(远侧同源盒 3)通过与骨形态发生蛋白(BMP)2 的正反馈环支持 DFCs 的成骨分化。然而,到目前为止,其他信号通路对这种 BMP2/DLX3 途径的控制仍不清楚。先前的研究还表明,NOTCH 信号通路在 DFCs 的成骨分化中起作用。在这项研究中,我们表明,DLX3 的过表达以及 BMP2 或地塞米松诱导的成骨分化起始诱导了 DFCs 中的 NOTCH 信号通路。然而,NOTCH 信号的诱导不仅损害了成骨分化(碱性磷酸酶活性和矿化结节),还损害了转录因子 DLX3 的表达和 BMP 信号通路的激活。因此,NOTCH 信号在 DFCs 的成骨分化中起调节作用。总之,我们的研究结果表明,在 DFCs 的成骨分化过程中激活的 NOTCH 信号通路通过负反馈环调节 DFCs 中 BMP2/DLX3 指导的分化。
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